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The emerging role of MCPH1/BRIT1 in carcinogenesis

The MCPH1 gene, also known as BRCT-repeat inhibitor of hTERT expression (BRIT1), has three BRCA1 carboxyl-terminal domains which is an important regulator of DNA repair, cell cycle checkpoints and chromosome condensation. MCPH1/BRIT1 is also known as a tumour suppressor in different types of human c...

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Autores principales: Alsolami, Mona, Aboalola, Doaa, Malibari, Dolal, Alghamdi, Tariq, Alshekhi, Walaa, Jad, Hind, Rumbold-Hall, Rea, Altowairqi, Ahlam S., Bell, Sandra M., Alsiary, Rawiah Abdullah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9951231/
https://www.ncbi.nlm.nih.gov/pubmed/36845691
http://dx.doi.org/10.3389/fonc.2023.1047588
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author Alsolami, Mona
Aboalola, Doaa
Malibari, Dolal
Alghamdi, Tariq
Alshekhi, Walaa
Jad, Hind
Rumbold-Hall, Rea
Altowairqi, Ahlam S.
Bell, Sandra M.
Alsiary, Rawiah Abdullah
author_facet Alsolami, Mona
Aboalola, Doaa
Malibari, Dolal
Alghamdi, Tariq
Alshekhi, Walaa
Jad, Hind
Rumbold-Hall, Rea
Altowairqi, Ahlam S.
Bell, Sandra M.
Alsiary, Rawiah Abdullah
author_sort Alsolami, Mona
collection PubMed
description The MCPH1 gene, also known as BRCT-repeat inhibitor of hTERT expression (BRIT1), has three BRCA1 carboxyl-terminal domains which is an important regulator of DNA repair, cell cycle checkpoints and chromosome condensation. MCPH1/BRIT1 is also known as a tumour suppressor in different types of human cancer. The expression level of the MCPH1/BRIT1 gene is decreased at the DNA, RNA or protein level in a number of types of cancers including breast cancer, lung cancer, cervical cancer, prostate cancer and ovarian cancer compared to normal tissue. This review also showed that deregulation of MCPH1/BRIT1 is significantly associated with reduced overall survival in 57% (12/21) and relapsed free survival in 33% (7/21) of cancer types especially in oesophageal squamous cell carcinoma and renal clear cell carcinoma. A common finding of this study is that the loss of MCPH1/BRIT1 gene expression plays a key role in promoting genome instability and mutations supporting its function as a tumour suppressor gene.
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spelling pubmed-99512312023-02-25 The emerging role of MCPH1/BRIT1 in carcinogenesis Alsolami, Mona Aboalola, Doaa Malibari, Dolal Alghamdi, Tariq Alshekhi, Walaa Jad, Hind Rumbold-Hall, Rea Altowairqi, Ahlam S. Bell, Sandra M. Alsiary, Rawiah Abdullah Front Oncol Oncology The MCPH1 gene, also known as BRCT-repeat inhibitor of hTERT expression (BRIT1), has three BRCA1 carboxyl-terminal domains which is an important regulator of DNA repair, cell cycle checkpoints and chromosome condensation. MCPH1/BRIT1 is also known as a tumour suppressor in different types of human cancer. The expression level of the MCPH1/BRIT1 gene is decreased at the DNA, RNA or protein level in a number of types of cancers including breast cancer, lung cancer, cervical cancer, prostate cancer and ovarian cancer compared to normal tissue. This review also showed that deregulation of MCPH1/BRIT1 is significantly associated with reduced overall survival in 57% (12/21) and relapsed free survival in 33% (7/21) of cancer types especially in oesophageal squamous cell carcinoma and renal clear cell carcinoma. A common finding of this study is that the loss of MCPH1/BRIT1 gene expression plays a key role in promoting genome instability and mutations supporting its function as a tumour suppressor gene. Frontiers Media S.A. 2023-01-31 /pmc/articles/PMC9951231/ /pubmed/36845691 http://dx.doi.org/10.3389/fonc.2023.1047588 Text en Copyright © 2023 Alsolami, Aboalola, Malibari, Alghamdi, Alshekhi, Jad, Rumbold-Hall, Altowairqi, Bell and Alsiary https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Alsolami, Mona
Aboalola, Doaa
Malibari, Dolal
Alghamdi, Tariq
Alshekhi, Walaa
Jad, Hind
Rumbold-Hall, Rea
Altowairqi, Ahlam S.
Bell, Sandra M.
Alsiary, Rawiah Abdullah
The emerging role of MCPH1/BRIT1 in carcinogenesis
title The emerging role of MCPH1/BRIT1 in carcinogenesis
title_full The emerging role of MCPH1/BRIT1 in carcinogenesis
title_fullStr The emerging role of MCPH1/BRIT1 in carcinogenesis
title_full_unstemmed The emerging role of MCPH1/BRIT1 in carcinogenesis
title_short The emerging role of MCPH1/BRIT1 in carcinogenesis
title_sort emerging role of mcph1/brit1 in carcinogenesis
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9951231/
https://www.ncbi.nlm.nih.gov/pubmed/36845691
http://dx.doi.org/10.3389/fonc.2023.1047588
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